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Find A Cure Transit Cystic Fibrosis Resources:
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The Blooming Rose Foundation was created to give hope to families immediately following diagnosis, fundraise to positively reach a vast array of individuals and offer an online resource for individuals, families, and friends to find up to date research, links to encouraging websites and blogs as well as a way to connect with other families and adults with CF.
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Making lives of those with Cystic Fibrosis easier one breath at a time. Breathe 4 Tomorrow is 501c3 that was founded to help families and patients living with Cystic Fibrosis with the extra costs that are associated with living with the disease. They help with utility bills, medical bills, lodging, gas and almost anything else that a family may need.
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CF Riders, along with our partner foundation, Laps for CF, is a non-profit organization based in Birmingham, AL dedicated to raising awareness of Cystic Fibrosis, and providing financial support in all areas of need for CF research, treatment, care, and improved quality of life.
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Pod cast hosted by Jerry Cahill
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The Cystic Fibrosis Institute (CFI) is committed to supporting those affected by cystic fibrosis in the Chicagoland area and to making a difference by being a meaningful and active source of assistance and advocacy for all CF individuals and families for dealing with the everyday challenge of cystic fibrosis.
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Dottie Lessard is a Personal Empowerment Coach, Nike Athlete, author and life inspiration to all she meets and has created a CF centric not profit called Dottie's Dream.
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Dr. Julie Desch established New Day Wellness (NDW) in 2005. NDW is a non-profit organization with the mission of providing health and wellness coaching and fitness training to individuals with chronic disease. Dr. Desch is a retired physician with cystic fibrosis who, at 46 years of age, has jumped enthusiastically into her second career
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Informational site created by Norma Plourde.
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Not a Wasted Breath is the story of how one man turned his obstacles into opportunities. Told from the viewpoint of a person who had cystic fibrosis and knew from an early age he would have a shortened life span, it contains his writings during his last four months of life as he waited in the hospital for a transplant that didn’t come in time; his story from his mother’s viewpoint; and reflections by nine persons impacted by his deep faith in God, his determination, his work ethic, and great sense of humor.
Find A Cure Transit Cystic Fibrosis Resources:
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